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Échelles pKHB et enthalpique du pouvoir accepteur de liaison hydrogène de thioéthers, thiols et disulfures
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/9780470171899.ch6openalex-snapshot
The Enthalpy‐Entropy Relationship
inferredcites →https://doi.org/10.1002/poc.437openalex-snapshot
An enthalpic scale of hydrogen‐bond basicity, part 1: halogenoalkanes
inferredcites →https://doi.org/10.1002/poc.652openalex-snapshot
An experimental and theoretical study of the preferred hydrogen bonding site of methyl isothiocyanate
inferredcites →https://doi.org/10.1002/poc.688openalex-snapshot
Determination of the hydrogen‐bond basicity of weak and multifunctional bases: the case of lindane (γ‐hexachlorocyclohexane)
inferredcites →https://doi.org/10.1007/978-3-642-85135-3openalex-snapshot
Hydrogen Bonding in Biological Structures
inferredcites →https://doi.org/10.1007/bfb0111213openalex-snapshot
The upsilon steric parameter — definition and determination
inferredcites →https://doi.org/10.1016/0013-4686(76)85034-7openalex-snapshot
Empirical parameters for donor and acceptor properties of solvents
inferredcites →https://doi.org/10.1016/0371-1951(61)80095-7openalex-snapshot
Infrared studies of hydrogen bonding in alcohol-base systems
inferredcites →https://doi.org/10.1016/0371-1951(64)80099-0openalex-snapshot
Hydrogen bonding studies—VIII. The thermodynamics of hydrogen bonding of phenol to some oxygen-containing molecules and to benzene
inferredcites →https://doi.org/10.1016/s0022-328x(00)87856-0openalex-snapshot
Basicity of siloxanes, alkoxysilanes and ethers toward hydrogen bonding
inferredcites →https://doi.org/10.1021/ci000089sopenalex-snapshot
A Program for Linear Regression with a Common Point of Intersection: The Isokinetic Relationship
inferredcites →https://doi.org/10.1021/cr00002a004openalex-snapshot
A survey of Hammett substituent constants and resonance and field parameters
inferredcites →https://doi.org/10.1021/ja00267a063openalex-snapshot
A scale of directional substituent polarizability parameters from ab initio calculations of polarizability potentials
inferredcites →https://doi.org/10.1021/ja00364a005openalex-snapshot
Absolute hardness: companion parameter to absolute electronegativity
inferredcites →https://doi.org/10.1021/ja00711a029openalex-snapshot
Hydrogen-bonded complex formation. III. Thermodynamics of complexing by infrared spectroscopy and calorimetry
inferredcites →https://doi.org/10.1021/ja00721a010openalex-snapshot
Hydrogen bonding of sulfur donors with various phenols
inferredcites →https://doi.org/10.1021/ja00761a010openalex-snapshot
Hydrogen bond interactions with sulfur donors
inferredcites →https://doi.org/10.1021/ja00819a028openalex-snapshot
Basicity. Comparison of hydrogen bonding and proton transfer to some Lewis bases
inferredcites →https://doi.org/10.1021/ja00875a062openalex-snapshot
The Relative Strengths of Alkyl Halides as Proton Acceptor Groups in Hydrogen Bonding
inferredcites →https://doi.org/10.1021/ja01008a002openalex-snapshot
Association of indole and phenol with diethyl chalcogenides
inferredcites →https://doi.org/10.1021/ja01045a038openalex-snapshot
Studies of hydrogen-bonded complex formation with p-fluorophenol. V. Linear free energy relationships with OH reference acids
inferredcites →https://doi.org/10.1021/ja01070a005openalex-snapshot
Hydrogen Bonding Studies. IX. The Thermodynamics of Hydrogen Bonding of Phenol to Ethers and Related Compounds
inferredcites →https://doi.org/10.1021/ja952871sopenalex-snapshot
Directionality of Hydrogen Bonds to Sulfur and Oxygen
inferredcites →https://doi.org/10.1021/jo00242a039openalex-snapshot
Studies on amphiprotic compounds. 3. Hydrogen-bonding basicity of oxygen and sulfur compounds
inferredcites →https://doi.org/10.1023/a:1008743229409openalex-snapshot
Observations on the strength of hydrogen bonding
inferredcites →https://doi.org/10.1039/a708362iopenalex-snapshot
Hydrogen bonding Part 44 Thermodynamics of complexation of 3,5-dichlorophenol with ketones and ethers in cyclohexane: the Badger–Bauer relationship
inferredcites →https://doi.org/10.1039/a901867kopenalex-snapshot
The first basicity scale of fluoro-, chloro-, bromo- and iodo-alkanes: some cross-comparisons with simple alkyl derivatives of other elements
inferredcites →https://doi.org/10.1039/ft9938902433openalex-snapshot
Hydrogen bonds between cholesterol and oxygen bases: a thermodynamic study
inferredcites →https://doi.org/10.1039/p29920002091openalex-snapshot
Hydrogen-bond basicity of secondary and tertiary amides, carbamates, ureas and lactams
inferredcites →https://doi.org/10.1039/p29950002075openalex-snapshot
Hydrogen-bond basicity of thioamides and thioureas
inferredcites →https://doi.org/10.1039/tf9666201056openalex-snapshot
Spectroscopic studies of hydrogen bonding in donor-acceptor systems
inferredcites →https://doi.org/10.1051/jcp/1978750063openalex-snapshot
Étude par spectroscopie d’absorption infrarouge de complexes d’association du cyclohexanol, en solution diluée dans le tétrachlorure de carbone : aspects thermodynamiques
inferredcites →https://doi.org/10.1063/1.1749952openalex-snapshot
Spectroscopic Studies of the Hydrogen Bond. II. The Shift of the O–H Vibrational Frequency in the Formation of the Hydrogen Bond
inferredcites →https://doi.org/10.1063/1.1750645openalex-snapshot
The Relation Between the Energy of a Hydrogen Bond and the Frequencies of the O–H Bands
inferredcites →https://doi.org/10.1107/s0108768197002656openalex-snapshot
Resonance-Induced Hydrogen Bonding at Sulfur Acceptors in R 1 R 2C=S and R 1CS2 − Systems
inferredcites →https://doi.org/10.1135/cccc19692390openalex-snapshot
Determination of thermodynamic functions by means of infrared spectroscopy. Complex formation in phenol-aliphatic sulfide and phenol-aliphatic sulfoxide systems
inferredcites →https://doi.org/10.1139/v02-176openalex-snapshot
L'échelle pKHB de basicité de liaison hydrogène des amines tertiaires aliphatiques
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4892996openalex-extracted
Can the hydrogen bonding enthalpy be calculated from the binding constant at 298.15 K?
inferred← citeshttps://doi.org/10.1002/9780470681909.ch4openalex-snapshot
Thermodynamic and Spectroscopic Scales of Hydrogen‐Bond Basicity and Affinity
inferred← citeshttps://doi.org/10.1002/asia.200700241openalex-snapshot
Highly Diastereoselective Friedel–Crafts Alkylation Reactions via Chiral α‐Functionalized Benzylic Carbocations
inferred← citeshttps://doi.org/10.1002/cctc.202400685openalex-snapshot
Selective Photocatalytic Oxidation of Thioethers to Sulfoxides Mediated by a Carbon Nanotube‐Porphyrin Nanohybrid
inferred← citeshttps://doi.org/10.1016/b978-008044992-0.00105-xopenalex-snapshot
Thiiranes and Thiirenes: Monocyclic
inferred← citeshttps://doi.org/10.1016/b978-008044992-0.00207-8openalex-snapshot
Thietanes and Thietes: Monocyclic
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2012.06.002openalex-snapshot
Tungsten carbonyl σ-complexes of nido-carborane thioethers
inferred← citeshttps://doi.org/10.1016/j.molliq.2024.125353openalex-snapshot
Can the hydrogen bonding enthalpy be calculated from the binding constant at 298.15 K?
inferred← citeshttps://doi.org/10.1016/j.molliq.2025.127053openalex-snapshot
The relationship between the Gibbs energies and enthalpies of hydrogen bonding and charge-transfer complex formation in non-electrolytes solutions. Is it a rule?
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.2c02586openalex-snapshot
Steric and Lewis Basicity Influence of the Second Coordination Sphere on Electrocatalytic CO2 Reduction by Manganese Bipyridyl Complexes
inferred← citeshttps://doi.org/10.1021/ja3018187openalex-snapshot
Stereoselective Assembly of Complex Oligosaccharides Using Anomeric Sulfonium Ions as Glycosyl Donors
inferred← citeshttps://doi.org/10.1021/jo050535gopenalex-snapshot
An Enthalpic Scale of Hydrogen-Bond Basicity. 3. Ammonia, Primary, Secondary, and Tertiary Amines
inferred← citeshttps://doi.org/10.1021/jo100461zopenalex-snapshot
An Enthalpic Scale of Hydrogen-Bond Basicity. 4. Carbon π Bases, Oxygen Bases, and Miscellaneous Second-Row, Third-Row, and Fourth-Row Bases and a Survey of the 4-Fluorophenol Affinity Scale
inferred← citeshttps://doi.org/10.1021/jp054173sopenalex-snapshot
B3LYP and MP2 Calculations of the Enthalpies of Hydrogen-Bonded Complexes of Methanol with Neutral Bases and Anions: Comparison with Experimental Data
inferred← citeshttps://doi.org/10.1021/jp2099976openalex-snapshot
Fluorine–Fluorine Interactions in the Solid State: An Experimental and Theoretical Study
inferred← citeshttps://doi.org/10.1080/10426507.2010.523035openalex-snapshot
Catalysis of Electrochemical Reduction of Weak Acids to Produce H2: Role of O‒H…S Hydrogen Bonding
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